US4908436A - Fibre-reactive azo dyes containing vinylsulfonyl groups and further aliphatic fibre-reactive radicals - Google Patents
Fibre-reactive azo dyes containing vinylsulfonyl groups and further aliphatic fibre-reactive radicals Download PDFInfo
- Publication number
- US4908436A US4908436A US06/921,849 US92184986A US4908436A US 4908436 A US4908436 A US 4908436A US 92184986 A US92184986 A US 92184986A US 4908436 A US4908436 A US 4908436A
- Authority
- US
- United States
- Prior art keywords
- amino
- benzene
- triazine
- chloro
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- -1 vinylsulfonyl groups Chemical group 0.000 title claims abstract description 154
- 239000000987 azo dye Substances 0.000 title description 2
- 125000001931 aliphatic group Chemical group 0.000 title 1
- 239000000985 reactive dye Substances 0.000 claims abstract description 52
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 27
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 23
- 239000000460 chlorine Substances 0.000 claims abstract description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 18
- 239000001257 hydrogen Substances 0.000 claims abstract description 18
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 15
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 14
- 239000011737 fluorine Substances 0.000 claims abstract description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 13
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 13
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 5
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims abstract description 5
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims abstract description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
- RJSYPKWVIJGNLO-UHFFFAOYSA-N CCOClOC Chemical group CCOClOC RJSYPKWVIJGNLO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000005118 N-alkylcarbamoyl group Chemical group 0.000 claims abstract description 3
- 125000004442 acylamino group Chemical group 0.000 claims abstract description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract 2
- 125000004957 naphthylene group Chemical group 0.000 claims abstract 2
- ZFDLFHQAGYPRBY-UHFFFAOYSA-N chloro acetate Chemical compound CC(=O)OCl ZFDLFHQAGYPRBY-UHFFFAOYSA-N 0.000 claims description 8
- 150000002431 hydrogen Chemical group 0.000 claims description 4
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 119
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 66
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 49
- 239000000243 solution Substances 0.000 description 48
- 239000000975 dye Substances 0.000 description 46
- 125000006125 ethylsulfonyl group Chemical group 0.000 description 44
- 150000003254 radicals Chemical class 0.000 description 40
- 229920000742 Cotton Polymers 0.000 description 30
- 239000002253 acid Substances 0.000 description 27
- 239000004744 fabric Substances 0.000 description 27
- 238000000034 method Methods 0.000 description 24
- 238000005859 coupling reaction Methods 0.000 description 23
- 238000004043 dyeing Methods 0.000 description 22
- 239000011541 reaction mixture Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 18
- 239000000543 intermediate Substances 0.000 description 18
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 17
- 230000008878 coupling Effects 0.000 description 16
- 238000010168 coupling process Methods 0.000 description 16
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 14
- 230000005494 condensation Effects 0.000 description 14
- 238000003379 elimination reaction Methods 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- XWBDWHCCBGMXKG-UHFFFAOYSA-N ethanamine;hydron;chloride Chemical compound Cl.CCN XWBDWHCCBGMXKG-UHFFFAOYSA-N 0.000 description 10
- VMKJWLXVLHBJNK-UHFFFAOYSA-N cyanuric fluoride Chemical compound FC1=NC(F)=NC(F)=N1 VMKJWLXVLHBJNK-UHFFFAOYSA-N 0.000 description 9
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 8
- APRRQJCCBSJQOQ-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S(O)(=O)=O)=CC2=C1 APRRQJCCBSJQOQ-UHFFFAOYSA-N 0.000 description 8
- DDUHZTYCFQRHIY-UHFFFAOYSA-N 7-chloro-3',4,6-trimethoxy-5'-methylspiro[1-benzofuran-2,4'-cyclohex-2-ene]-1',3-dione Chemical compound COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- 238000009833 condensation Methods 0.000 description 8
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 230000007935 neutral effect Effects 0.000 description 8
- 239000002243 precursor Substances 0.000 description 8
- PYNUOAIJIQGACY-UHFFFAOYSA-N propylazanium;chloride Chemical compound Cl.CCCN PYNUOAIJIQGACY-UHFFFAOYSA-N 0.000 description 8
- KVAQXZADNRRNCK-UHFFFAOYSA-N 2-(2-chloroethylsulfonyl)ethanamine;hydrochloride Chemical compound Cl.NCCS(=O)(=O)CCCl KVAQXZADNRRNCK-UHFFFAOYSA-N 0.000 description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000006482 condensation reaction Methods 0.000 description 6
- 239000003599 detergent Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- ZUQOBHTUMCEQBG-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-1,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(O)=C2C(N)=CC=C(S(O)(=O)=O)C2=C1 ZUQOBHTUMCEQBG-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 230000008030 elimination Effects 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
- JVMSQRAXNZPDHF-UHFFFAOYSA-N 2,4-diaminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C(N)=C1 JVMSQRAXNZPDHF-UHFFFAOYSA-N 0.000 description 3
- JXOVOQXOYUTSGF-UHFFFAOYSA-N ClC1=NC=NC(N(CCS(=O)(=O)C=C)CCS(=O)(=O)C=C)=N1 Chemical compound ClC1=NC=NC(N(CCS(=O)(=O)C=C)CCS(=O)(=O)C=C)=N1 JXOVOQXOYUTSGF-UHFFFAOYSA-N 0.000 description 3
- SYYVQEUGBQMUFH-UHFFFAOYSA-N ClC1=NC=NC(NCCS(=O)(=O)C=C)=N1 Chemical compound ClC1=NC=NC(NCCS(=O)(=O)C=C)=N1 SYYVQEUGBQMUFH-UHFFFAOYSA-N 0.000 description 3
- LKGLAHMDUILPRX-UHFFFAOYSA-N FC1=NC=NC(N(CCS(=O)(=O)C=C)CCS(=O)(=O)C=C)=N1 Chemical compound FC1=NC=NC(N(CCS(=O)(=O)C=C)CCS(=O)(=O)C=C)=N1 LKGLAHMDUILPRX-UHFFFAOYSA-N 0.000 description 3
- FDGSVKYHRGZFSO-UHFFFAOYSA-N FC1=NC=NC(NCCS(=O)(=O)C=C)=N1 Chemical compound FC1=NC=NC(NCCS(=O)(=O)C=C)=N1 FDGSVKYHRGZFSO-UHFFFAOYSA-N 0.000 description 3
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000012433 hydrogen halide Substances 0.000 description 3
- 229910000039 hydrogen halide Inorganic materials 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000001103 potassium chloride Substances 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 description 3
- 230000019635 sulfation Effects 0.000 description 3
- 238000005670 sulfation reaction Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- UGEHFOSBNBEWMP-UHFFFAOYSA-N 2,3-diaminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1N UGEHFOSBNBEWMP-UHFFFAOYSA-N 0.000 description 2
- LNKCXUFJUDPYLP-UHFFFAOYSA-N 2-(2-chloroethylsulfonyl)-n-[2-(2-chloroethylsulfonyl)ethyl]ethanamine Chemical compound ClCCS(=O)(=O)CCNCCS(=O)(=O)CCCl LNKCXUFJUDPYLP-UHFFFAOYSA-N 0.000 description 2
- HPKMXOWNGSBOME-UHFFFAOYSA-N 2-(2-chloroethylsulfonyl)ethanamine Chemical compound NCCS(=O)(=O)CCCl HPKMXOWNGSBOME-UHFFFAOYSA-N 0.000 description 2
- UPFQSSFFSZYHHE-UHFFFAOYSA-N 2-amino-4-[[4-chloro-6-(2-ethenylsulfonylethylamino)-1,3,5-triazin-2-yl]amino]benzenesulfonic acid Chemical compound C1=C(S(O)(=O)=O)C(N)=CC(NC=2N=C(NCCS(=O)(=O)C=C)N=C(Cl)N=2)=C1 UPFQSSFFSZYHHE-UHFFFAOYSA-N 0.000 description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 2
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
- LDQMZKBIBRAZEA-UHFFFAOYSA-N 4-amino-2-aminobenzoic acid Natural products NC1=CC=C(C(O)=O)C(N)=C1 LDQMZKBIBRAZEA-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- CRIKLGDHCZEWBP-UHFFFAOYSA-N [Cl-].C(C)[NH3+].C1=CC=CC=C1 Chemical compound [Cl-].C(C)[NH3+].C1=CC=CC=C1 CRIKLGDHCZEWBP-UHFFFAOYSA-N 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 150000001266 acyl halides Chemical class 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- OPZGHHMHHWXKAA-UHFFFAOYSA-N benzenesulfonic acid;hydrochloride Chemical compound Cl.OS(=O)(=O)C1=CC=CC=C1 OPZGHHMHHWXKAA-UHFFFAOYSA-N 0.000 description 2
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical group C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 2
- 150000004696 coordination complex Chemical class 0.000 description 2
- 150000004985 diamines Chemical group 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 238000009775 high-speed stirring Methods 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- RBORURQQJIQWBS-QVRNUERCSA-N (4ar,6r,7r,7as)-6-(6-amino-8-bromopurin-9-yl)-2-hydroxy-2-sulfanylidene-4a,6,7,7a-tetrahydro-4h-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol Chemical compound C([C@H]1O2)OP(O)(=S)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1Br RBORURQQJIQWBS-QVRNUERCSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- AZXGXVQWEUFULR-UHFFFAOYSA-N 2',4',5',7'-tetrabromofluorescein Chemical compound OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 AZXGXVQWEUFULR-UHFFFAOYSA-N 0.000 description 1
- WCZNKVPCIFMXEQ-UHFFFAOYSA-N 2,3,5,6-tetramethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=C(C)C(C)=C1N WCZNKVPCIFMXEQ-UHFFFAOYSA-N 0.000 description 1
- NAWJZCSEYBQUGY-UHFFFAOYSA-N 2,3-diaminobenzamide Chemical compound NC(=O)C1=CC=CC(N)=C1N NAWJZCSEYBQUGY-UHFFFAOYSA-N 0.000 description 1
- HWKWYDXHMQQDQJ-UHFFFAOYSA-N 2,3-dibromopropanoyl chloride Chemical compound ClC(=O)C(Br)CBr HWKWYDXHMQQDQJ-UHFFFAOYSA-N 0.000 description 1
- ZVDSMYGTJDFNHN-UHFFFAOYSA-N 2,4,6-trimethylbenzene-1,3-diamine Chemical compound CC1=CC(C)=C(N)C(C)=C1N ZVDSMYGTJDFNHN-UHFFFAOYSA-N 0.000 description 1
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 description 1
- XAQCYASNAMYTQA-UHFFFAOYSA-N 2,4-diamino-5-methylbenzenesulfonic acid Chemical compound CC1=CC(S(O)(=O)=O)=C(N)C=C1N XAQCYASNAMYTQA-UHFFFAOYSA-N 0.000 description 1
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- BIYQLXLSSLKTNE-UHFFFAOYSA-N n-(3-aminophenyl)-2-hydroxyacetamide Chemical compound NC1=CC=CC(NC(=O)CO)=C1 BIYQLXLSSLKTNE-UHFFFAOYSA-N 0.000 description 1
- PEMGGJDINLGTON-UHFFFAOYSA-N n-(3-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=CC(N)=C1 PEMGGJDINLGTON-UHFFFAOYSA-N 0.000 description 1
- GOGZBMRXLADNEV-UHFFFAOYSA-N naphthalene-2,6-diamine Chemical compound C1=C(N)C=CC2=CC(N)=CC=C21 GOGZBMRXLADNEV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 238000009980 pad dyeing Methods 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/4401—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
- C09B62/4411—Azo dyes
Definitions
- the present invention relates to novel reactive dyes, to a process for their preparation, and to their use for dyeing and printing fibre materials.
- the object of the present invention to provide new, improved reactive dyes for the cold pad-batch method which have the qualities characterised above to a high degree.
- the new dyes should be distinguished especially by high degrees of fixation and high fibre-dye bond stabilities, and the unfixed portions on the fibre should moreover be readily washed off. They should also produce dyeings having good all-round fastness properties, for example light and wet fastness properties.
- the invention accordingly provides reactive dyes of the formula ##STR4## in which D, D 1 and D 2 are each a phenylene or naphthylene radical which can be further substituted, R 1 is hydrogen or substituted or unsubstituted C 1-4 -alkyl, R 2 is hydrogen, substituted or unsubstituted alkyl or aryl or a radical of the formula --alk--SO 2 --Z, E --NH 2 , --CH 3 , --NH--CO--NH 2 , --NH--CO--CH 3 or --NH--CO--CH 2 --OH, alk is C 2-6 -alkylene, Y is a --SO 2 --Z, --SO 2 --N(R 1 )--Z, --N(R 1 )--SO 2 --Z, ##STR5## --SO 2 --F, --SO 2 --CH 2 --CH ⁇ CH 2 , --N(R 1 )--CO--CBr ⁇ CH 2 , --N(R 1 )-
- radicals D, D 1 and D 2 in the formulae (1), (2) and (2a) can be further substituted in conventional manner.
- further substituents are alkyl groups having 1 to 4 carbon atoms, such as methyl, ethyl, propyl, isopropyl or butyl, alkoxy groups having 1 to 4 carbon atoms, such as methoxy, ethoxy, propoxy, isopropoxy or butoxy, acylamino groups having 1 to 8 carbon atoms, such as acetylamino, propionylamino or benzoylamino, amino, alkylamino having 1 to 4 carbon atoms, such as methylamino, ethylamino, propylamino, isopropylamino or butylamino, phenylamino, N,N-di- ⁇ -hydroxyethylamino, N,N-di- ⁇ -sulfatoethylamino, sulfobenzylamino
- Preferred further substituents are methyl, ethyl, methoxy, ethoxy, acetylamino, benzoylamino, amino, chlorine, bromine, ureido, hydroxyl, carboxyl, sulfomethyl and sulfur.
- the radicals D, D 1 and D 2 preferably contain one or more sulfo groups.
- the alkyl radical R 1 can be straight-chain or branched and can also be further substituted, for example by halogen, hydroxyl, cyano, C 1-4 -alkoxy, carboxyl or sulfo.
- R 1 are: methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec.-butyl, tert.-butyl, carboxymethyl, ⁇ -carboxyethyl, ⁇ -carboxypropyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, ⁇ -methoxyethyl, ⁇ -ethoxyethyl, ⁇ -methoxypropyl, ⁇ -chloroethyl, ⁇ -bromopropyl, ⁇ -hydroxyethyl, ⁇ -hydroxybutyl, ⁇ -cyanoethyl, sulfomethyl, ⁇ -sulfoethyl, aminosulf
- the radical R 2 can be for example an alkyl radical which is straight-chain or branched, which preferably has 1 to 6 carbon atoms and which can be further substituted, for example by halogen, hydroxyl, cyano, alkoxy, carboxyl or sulfo, or an unsubstituted alkyl radical having 7 to 20 carbon atoms, a cyclohexyl radical, or a phenyl radical which can be substituted, for example by methyl, ethyl, methoxy, ethoxy, chlorine, bromine, carboxyl, sulfo or sulfomethyl.
- R 2 are the following substituents: methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec.-butyl, tert.-butyl, pentyl, hexyl, nonyl, dodecyl, hexadecyl, pentadecyl, carboxymethyl, ⁇ -carboxyethyl, ⁇ -carboxypropyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, ⁇ -methoxyethyl, ⁇ -ethoxyethyl, ⁇ -methoxypropyl, ⁇ -chloroethyl, ⁇ -chloropropyl, ⁇ -bromopropyl, sulfomethyl, ⁇ -sulfoethyl, aminosulfonylmethyl, ⁇ -sulfatoethyl, cyclohexyl, phenyl, o-
- R 2 is a radical of the formula --alk--SO 2 --Z
- the two radicals which are bonded to the nitrogen atom in question can be identical or different.
- the two radicals of the formula --alk--SO 2 --Z are preferably identical.
- the bridge member alk is a straight-chain or branched alkylene radical having 2 to 6 carbon atoms, for example ethylene, n-propylene, isopropylene, n-butylene, n-pentylene or n-hexylene. alk is preferably an ethylene radical.
- the inorganic or organic radical which can be detached under alkaline conditions can be one of the following anionically detachable groups: ##STR6##
- Y examples are ⁇ -sulfatoethylsulfonyl, vinylsulfonyl, ⁇ -sulfatoethylaminosulfonyl, N-methyl-N- ⁇ -sulfatoethylaminosulfonyl, N-ethyl-N- ⁇ -sulfatoethylaminosulfonyl, ⁇ -chloroethylsulfonyl, chloroacetylamino, ⁇ , ⁇ -dichloropropionylamino, ⁇ , ⁇ -dibromopropionylamino, ⁇ -bromoacryloylamino and 4-( ⁇ -chloroethylsulfonyl)-butyrylamino.
- Y is preferably sulfatoethylsulfonyl or vinylsulfonyl.
- radical --N(R 2 )--alk--SO 2 --Z examples are ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamino, ⁇ -( ⁇ -chloroethylsulfonyl)-propylamino, bis-[ ⁇ -( ⁇ -chloroethylsulfonyl)-ethyl]-amino, N-methyl-N- ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamino, N-phenyl-N- ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamino, ⁇ -vinylsulfonyl-ethylamino, bis( ⁇ -vinylsulfonyl-ethyl)-amino, N- ⁇ -sulfatoethyl-N- ⁇ -( ⁇ -chloroethylsulfonyl
- the substituent X is in particular chlorine and especially fluorine.
- the process for preparing the reactive dyes of the formulae (1), (2) or (2a) comprises reacting dyes of the formulae ##STR12## or their precursors with reactive components to introduce the radicals of the formula ##STR13## to give reactive dyes of the formula (1), (2) or (2a), or converting the intermediates obtained into the desired end dyes, and if desired immediately carrying out a further conversion.
- radical Y and of the radical of the formula (12) into the dye of the formula (10), (10a) or (11) is effected in a manner known per se, for example through acylation with appropriate carboxylic acid halides or anhydrides and condensation with cyanuric halides and amines of the formula
- Y is a radical which is bonded via a --N(R 1 )-- amino group
- D or D 1 must contain such an amino group.
- the diazo component is a diamine or a corresponding amino acetylamino or amino nitro compound in which the acetylamino and nitro groups are converted before the condensation with the acylating agent into the NH 2 group by hydrolysis and reduction respectively.
- Y is a directly bonded sulfonyl radical
- the starting material used is a precursor which already contains this radical, for example 1-amino-4- ⁇ -sulfatoethylsulfonylbenzene as diazo component.
- the reactions required for preparing the end dyes from precursors are couplings or conversions to the reactive radicals.
- a diazo component which contains an acylatable --N(R 1 )H group is acylated with an acyl halide
- the reaction product is diazotised and coupled onto a coupling component which contains a --N(R 1 )H group
- the resulting monoazo compound is condensed with an aminodihalogenotriazine of the formula ##STR14## in which X is fluorine or chlorine or acylated with a trihalogeno-s-triazine, and the product is subsequently condensed with an amine of the formula (13).
- Another method comprises first of all preparing a dye which contains a precursor of the reactive radical and then converting this precursor into the reactive radical itself, for example by esterification or an addition reaction.
- a dye in which Y contains an HO--CH 2 CH 2 -- radical and to react the intermediate before or after the acylation with sulfuric acid, so that the hydroxyl group is converted into the sulfato group; or to use an analogous dye in which Y contains the H 2 C ⁇ CH-- vinyl group, and to add the intermediate onto thiosulfuric acid, producing an HO 3 SS--CH 2 CH 2 -- radical.
- the hydroxyl group in a dye of the formula (10) or (11) or in a suitable precursor is preferably sulfated by reaction at 0° C. to moderately elevated temperatures with concentrated sulfuric acid.
- This sulfation can also be effected by reacting the hydroxy compound at 10° to 80° C. with 2 equivalents of chlorosulfonic acid per hydroxyl group in a polar organic solvent, for example N-methylpyrrolidone.
- the sulfation is preferably effected by adding the compound in question to sulfuric acid monohydrate at temperatures between 5° and 15° C. In the subsequent sulfation a fluorine atom on the triazine ring can be replaced by a hydroxyl group.
- reactive dyes of the formula (1) which contain sulfatoethylsulfonyl radicals can be treated with agents which eliminate hydrogen halide, such as sodium hydroxide, to convert the sulfatoethylsulfonyl radicals into vinylsulfonyl radicals.
- the radical Y is an ⁇ , ⁇ -dibromopropionylamino radical
- the ⁇ , ⁇ -dibromopropionyl group by treatment with agents which eliminate hydrogen halide, can be converted into the ⁇ -bromoacryloyl group, if desired at the same time as the abovementioned elimination of sulfuric acid from a sulfatoethylsulfonyl radical.
- the dyes of the formulae (10) or (11) or the dye precursors are acylated with acyl halides or halogenotriazines in manners known per se, preferably in aqueous solutions or suspensions and in the presence of alkaline, acid-binding agents, for example aqueous alkali metal hydroxides, carbonates or bicarbonates.
- Reactive dyes of the formula (1) in which Y is a directly bonded sulfonyl radical can be prepared by starting from dyes of the formulae (10) or (11) which already contain a Y group, and acylating the --N(R 1 )H group with a halogenotriazine, or using appropriate precursors, for example a diazo component of the formula ##STR15## and coupling it onto a coupling component which contains a --N(R 1 )H group, and acylating the --N(R 1 )H group with a halogenotriazine before or after the coupling.
- the reactive dyes contain groups capable of metal complex formation, the reactive dyes can also be subsequently metallised.
- the diazo component to be used is not a diamine but an aminoacetylamino compound from which the acetyl is subsequently to be reeliminated by hydrolysis, as mentioned above in the description of the process variants, the monoacetyl compounds of the abovementioned diazo compounds are possible, examples being 1-acetylamino-3-aminobenzene-4-sulfonic acid and 1-acetylamino-4-aminobenzene-3-sulfonic acid.
- diazo components which already contain a Y group are 1-amino-2-, -3- or -4- ⁇ -sulfoethylsulfonylbenzene, 1-amino-3- ⁇ -phosphatoethylsulfonylbenzene, 1-amino-4-methyl-3- ⁇ -sulfatoethylsulfonylbenzene, 1-amino-3- ⁇ -chloroethylsulfonylbenzene, 1-amino-4-methoxy-3- ⁇ -sulfatoethylsulfonylbenzene, 1-amino-4- ⁇ -sulfatoethylsulfonylbenzene-2-sulfonic acid, 1-amino-5- ⁇ -sulfatoethylsulfonylbenzene-2-sulfonic acid, 1-amino-5- ⁇ -sulfatoethylsulfonylbenzene-2,4-disul
- halides of the abovementioned Y radicals for example ⁇ , ⁇ -dibromopropionyl chloride, ⁇ , ⁇ -dichloropropionyl chloride, ⁇ -bromoacryloyl chloride or ⁇ -chloroacryloyl chloride, if desired also similarly reacting halogenated anhydrides, such as ⁇ , ⁇ -dichloropropionic anhydride, 4-( ⁇ -chloroethylsulfonyl)-butyryl chloride, 4-vinylsulfonylbutyryl chloride and the like, 2,4,6-trifluoro-s-triazine (cyanuric fluoride) and 2,4,6-trichloro-s-triazine (cyanuric chloride), as well as the primary condensation products of 2,4,6-trifluoro-s-triazine or 2,4,6-trichloro-s-triazine with the amines of the formula (13) mentioned hereinafter.
- amines of low molecular weight such as ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamine and its N-methyl derivative.
- Bis-[ ⁇ -( ⁇ -chloroethylsulfonyl)-ethyl]-amine is particularly preferred.
- Examples of possible dyes of the formulae (10) and (11) are dyes of the following structural groups: ##STR16## metal complexes of dyes of the formulae ##STR17##
- the metal atom is preferably Cu (1:1 complex) or Cr and Co (1:2 complex).
- Cr- and Co-complexes can contain one or two molecules of the azo compound of the abovementioned formula, i.e. they can be symmetrical or include any other ligand group and be asymmetrical.
- the fused rings indicated by the broken lines stand for alternatively possible naphthalene systems.
- the dyes of the abovementioned formulae can be further substituted in the alkyl or aryl radicals, in particular by the substituents mentioned in the explanation of the formula (1). ##STR19## and the metal complex azo dyes of the formulae ##STR20##
- the diazotisation of the diazo components and of the intermediates containing a diazotisable amino group is generally effected through the action of nitrous acid in aqueous mineral acid solutions at low temperatures.
- the coupling onto the coupling component is effected at strongly acid, neutral or weakly alkaline pH.
- the condensation of the reactive components with the diazo components and coupling components and with the amines or with acylatable monoazo or disazo intermediates or with the amino-containing dyes is preferably effected in aqueous solutions or suspensions, at low temperatures and at weakly acid, neutral or weakly alkaline pH.
- the hydrogen halide set free in the course of the condensation is advantageously continuously neutralised by adding aqueous alkali metal hydroxides, carbonates or bicarbonates.
- the reactive dyes of the formula (1) are fibre-reactive.
- Fibre-reactive compounds are to be understood as meaning compounds which are capable of reacting with the hydroxyl groups of the cellulose or with the amino groups of natural or synthetic polyamides to form covalent chemical bonds.
- the reactive dyes of the formula (1) are suitable for dyeing and printing a very wide variety of different materials, such as silk, leather, wool, nylon fibres and polyurethanes, and in particular cellulose-containing fibre materials of any kind. Examples of these fibre materials are natural cellulose fibres, such as cotton, linen and hemp, pulp and regenerated cellulose.
- the reactive dyes of the formula (1) are also suitable for dyeing or printing hydroxyl-containing fibres present in blend fabrics, for example blends of cotton with polyester fibres or nylon fibres.
- the dyes according to the invention can be applied to the fibre material, and be fixed on the fibre, by various methods, in particular in the form of aqueous dye solutions and print pastes. They are suitable not only for the exhaust method but also for dyeing by the pad-dyeing method, whereby the cloth is impregnated with aqueous dye solutions which can contain salt, and the dyes are fixed after an alkali treatment or in the presence of alkali, if desired under heat. They are particularly suitable for the so-called cold pad-batch method, whereby the dye is applied on the pad-mangle together with the alkali and is then fixed by leaving the padded cloth to stand at room temperature for several hours. After the dye has been fixed the dyeings or prints are thoroughly rinsed with cold and hot water in the presence or absence of an agent which acts like a dispersant and promotes the diffusion of the unfixed portions.
- the reactive dyes of the formula (1) are distinguished by high reactivity and good fixing properties. For this reason they can be used for exhaust dyeing at low dyeing temperatures and only short steaming times are necessary in the pad-steam process.
- the degrees of fixation are high, and the unfixed portions are readily washed off, the difference between the degree of exhaustion and degree of fixation being remarkably small, i.e. the hydrolysis loss is very small.
- the reactive dyes of the formula (1) are also suitable for printing, in particular on cotton, but also for printing nitrogen-containing fibres, for example wool, silk or wool-containing blend fabrics.
- the dyeings and prints prepared with the dyes according to the invention on cellulose fibre materials have a high tinctorial strength and a high fibre-dye bond stability, both in the acid range and the alkaline range, plus a good light fastness and very good wet fastness properties, such as wash, water, seawater, cross-dyeing and perspiration fastness properties, and good pleating fastness, hot-press fastness and rub fastness.
- this dye intermediate is coupled at 0° to 10° C. and pH 6.0 with 28.1 parts of diazotised 1-amino-4-( ⁇ -sulfatoethylsulfonyl)-benzene.
- the reaction mixture is clarified and the resulting reactive dye of the formula ##STR21## is salted out by sprinkling in potassium chloride, is filtered off and is dried in vacuo. It dyes cotton in red shades.
- the isolation of the dye at pH 6.5-7.5 can be preceded by an elimination reaction in which the reaction solution is held at 15° to 25° C. at pH 9.0-10.0 by the continuous addition of 2N sodium hydroxide solution until complete conversion is indicated by chromatography.
- This intermediate is coupled at 0° to 10° C. and pH 1.0 with 28.1 parts of diazotised 1-amino-4-( ⁇ -sulfatoethylsulfonyl)-benzene. After the coupling reaction at pH 6.5 has ended, the reaction solution is brought to pH 8.0.
- the temperature of the reaction mixture is gradually raised from 5° C. to 20° C., while the reaction mixture is initially held at pH 6.5 and then at pH 8.0 by the continuous addition of 2N sodium hydroxide solution.
- the resulting reactive dye of the formula ##STR22## is salted out by sprinkling in potassium chloride at pH 7.0, is filtered off and is dried in vacuo. It dyes cotton in red shades.
- the dyes in Table 1 can also be synthesised analogously to this variant of the preparation.
- reaction mixture After the addition of 11.4 parts of ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamine hydrochloride, the reaction mixture is initially held briefly at pH 6.0 and then at pH 8.0 by the continuous addition of 2N sodium hydroxide solution while the temperature is raised from 20° to 25° C. in the course of 2 to 3 hours. After the condensation and elimination reaction has ended this dye intermediate is coupled at 0° to 10° C. and pH 6.0 with 14.1 L parts of diazotised 1-amino-(4-( ⁇ -sulfatoethylsulfonyl)-benzene. After the coupling reaction has ended at pH 6.5, the reaction mixture is held at pH 9.0 at 20° C.
- a mixture of 28.1 parts of diazotised 1-amino-4-( ⁇ -sulfatoethylsulfonyl)-benzene and 300 parts of water is added at 0° to 5° C. to 76.5 parts, dissolved in 600 parts of water, of the coupling component of the formula ##STR24## (prepared by acid coupling of diazotised 2-(3'-amino-4'-sulfophenylamino)-4-chloro-6-( ⁇ -vinylsulfonylethylamino)-1,3,5-triazine, prepared as described hereinafter, onto 1-amino-8-hydroxynaphthalene-3,6-disulfonic acid).
- the reaction mixture After the coupling reaction at pH 6.5 has ended, the reaction mixture, at 20° C., is held at pH 10.0 by the continuous addition of 2N sodium hydroxide solution until the complete elimination is indicated by chromatography. Thereafter of the reaction mixture is clarified at pH 6.5 and the synthesised dye of the formula ##STR25## is salted out by sprinkling in sodium chloride, is filtered off and is dried in vacuo. It dyes cotton in greenish blue shades.
- This intermediate is coupled at 0° to 10° C. and pH 1.0 with 28.1 parts of diazotised 1-amino-4-( ⁇ -sulfatoethylsulfonyl)-benzene. After the coupling reaction at pH 6.5 has ended, the reaction solution is brought pH 8.0.
- the temperature of the reaction mixture is gradually raised from 5° C. to 20° C., while the reaction mixture is initially held at pH 6.5 and then at pH 8.0 by the continuous addition of 2N sodium hydroxide solution.
- the resulting reactive dye of the formula ##STR26## is salted out by sprinkling in potassium chloride at pH 7.0, is filtered off and is dried in vacuo. It dyes cotton in red shades.
- reaction mixture After the addition of 11.4 parts of ⁇ -( ⁇ -chloroethylsulfonyl)-ethylamine hydrochloride, the reaction mixture is initially held briefly at pH 6.0 and then at pH 8.0 by the continuous addition of 2N sodium hydroxide solution while the temperature is raised from 20° to 25° C. in the course of 2 to 3 hours. After the condensation and elimination reaction has ended, this dye intermediate is coupled at 0° to 10° C. and pH 6.0 with 14.1 parts of diazotised 1-amino-(4-( ⁇ -sulfatoethylsulfonyl)-benzene. After the coupling reaction has ended at pH 6.5, the reaction mixture is held at pH 9.0 at 20° C.
- Example 2 parts of the dye obtained in Example 1 are dissolved in 400 parts of water; to this solution are added 1,500 parts of a solution which contains per liter 53 g of sodium chloride.
- 100 parts of a cotton fabric are introduced at 40° C. into this dyebath.
- 100 parts of a solution which contains per liter 16 g of sodium hydroxide and 20 g of calcined sodium carbonate are added.
- the temperature of the dyebath is held at 40° C. for a further 45 minutes.
- the dyed fabric is then rinsed, is soaped off at the boil with a nonionic detergent for a quarter of an hour, is rinsed once more and is dried.
- Example 2 parts of the reactive dye obtained in Example 1 are dissolved in 400 parts of water; to this solution are added 1,500 parts of a solution which contains per liter 53 g of sodium chloride.
- 100 parts of a cotton fabric are introduced at 35° C. into this dyebath.
- 100 parts of a solution which contains per liter 16 g of sodium hydroxide and 20 g of calcined sodium carbonate are added.
- the temperature of the dyebath is held at 35° C. for a further 15 minutes.
- the temperature is then raised to 60° C. in the course of 20 minutes.
- the temperature is held at 60° C. for a further 35 minutes.
- the fabric is then rinsed, is soaped off at the boil with a nonionic detergent for a quarter of an hour, is rinsed once more and is dried.
- Example 2 8 parts of the reactive dye obtained in Example 1 are dissolved in 400 parts of water; to this solution are added 1,400 parts of a solution which contains per liter 100 g of sodium sulfate. 100 parts of a cotton fabric are introduced at 25° C. into this dyebath. After 10 minutes 200 parts of a solution which contains per liter 150 g of trisodium phosphate are added. The temperature of the dyebath is then raised to 60° C. in the course of 10 minutes. The temperature is held at 60° C. for a further 90 minutes. The fabric is then rinsed, is soaped off at the boil with a nonionic detergent for a quarter of an hour, is rinsed once more and is dried.
- Example 2 4 parts of the reactive dye obtained in Example 1 are dissolved in 50 parts of water; to this solution are added 50 parts of a solution which contains per liter 5 g of sodium hydroxide and 20 g of calcined sodium carbonate.
- the resulting solution is applied to a cotton fabric on a pad-mangle in such a way that its weight increases by 70%, and the fabric is then wound onto a beam. In this state the cotton fabric is left to stand at room temperature for 3 hours.
- the dyed fabric is then rinsed, is soaped off at the boil with a nonionic detergent for a quarter of an hour, is rinsed once more and is dried.
- Example 2 6 parts of the reactive dye obtained in Example 1 are dissolved in 50 parts of water; to this solution are added 50 parts of a solution which contains per liter 16 g of sodium hydroxide and 0.04 liter of 38° Be sodium silicate.
- the resulting solution is applied to a cotton fabric on a pad-mangle in such a way that its weight increases by 70%, and the fabric is then wound onto a beam. In this state the cotton fabric is left at room temperature for 10 hours.
- the dyed fabric is then rinsed, is soaped off at the boil with a nonionic detergent for a quarter of an hour, is rinsed once more and is dried.
- Example 2 parts of the reactive dye obtained in Example 1 are dissolved in 100 parts of water in the presence of 0.5 part of sodium m-nitrobenzenesulfonate.
- the resulting solution is used to impregnate a cotton fabric in such a way that its weight increases by 75%, and the fabric is then dried.
- the fabric is then impregnated with a warm solution at 20° C. which contains per liter 4 g of sodium hydroxide and 300 g of sodium chloride, and is squeezed to a 75% weight increase and the dyeing is steamed at 100° to 102° C. for 30 seconds, is rinsed, is soaped off at the boil with a 0.3% strength solution of a nonionic detergent for a quarter of an hour, is rinsed and is dried.
- Example 3 parts of the reactive dye obtained in Example 1 are sprinkled with high-speed stirring into 100 parts of stock thickening containing 50 parts of 5% strength sodium alginate thickening, 27.8 parts of water, 20 parts of urea, 1 part of sodium m-nitrobenzenesulfonate and 1.2 parts of sodium hydrogencarbonate.
- the print paste thus obtained is used to print a cotton fabric, which is then dried, and the resulting printed fabric is steamed at 102° C. in saturated steam for 2 minutes.
- the printed fabric is then rinsed, if desired soaped off at the boil and rinsed once more, and is then dried.
- Example 1 5 parts of the reactive dye obtained in Example 1 are sprinkled with high-speed stirring into 100 parts of a stock thickening containing 50 parts of 5% strength sodium alginate thickening, 36.5 parts of water, 10 parts of urea, 1 part of sodium m-nitrobenzenesulfonate and 2.5 parts of sodium hydrogencarbonate.
- the print paste thus obtained whose stability meets industrial requirements, is used to print a cotton fabric, which is then dried, and the resulting printed fabric is steamed at 102° C. in saturated steam for 8 minutes. The printed fabric is then rinsed, if desired soaped off at the boil and rinsed once more, and is then dried.
Landscapes
- Chemical & Material Sciences (AREA)
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Abstract
Description
HN(R.sub.2)--alk--SO.sub.2 --Z (13).
TABLE 1
__________________________________________________________________________
Hue on
No.
Amino compound
Diazo component
cotton
__________________________________________________________________________
1 β-(β-Chloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
ethylamine hydrochloride
sulfonyl)-benzene
red
2 β-(β-Chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl-
red
ethylamine hydrochloride
sulfonyl)-benzene
3 β-(β-Chloroethylsulfonyl)-
1-amino-4-allylsulfonyl-
red
ethylamine hydrochloride
benzene
4 β-(β-Chloroethylsulfonyl)-
1-amino5-(2,3-dibromo-
yellowish
ethylamine hydrochloride
propionylamino)-benzene-
red
2-sulfonic acid
5 β-(β-Chloroethylsulfonyl)-
1-amino-5-(α-bromoacryloyl-
yellowish
ethylamine hydrochloride
amino)-benzene-2-sulfonic
red
acid
6 β-(β-Chloroethylsulfonyl)-
1-amino-5-(2,3-dichloro-
yellowish
ethylamine hydrochloride
propionylamino)-benzene-2-
red
sulfonic acid
7 β-(β-Chloroethylsulfonyl)-
1-amino-5-chloroacetylamino-
yellowish
ethylamine hydrochloride
benzene-2-sulfonic acid
red
8 Bis-(β-(β-chloroethyl-
1-amino-4-(β-sulfatoethyl-
red
sulfonyl)-ethyl)-amine
sulfonyl)-benzene
hydrochloric acid
9 Bis-(β-(β-chloroethyl-
1-amino-2-(β-sulfatoethyl-
red
sulfonyl)-ethyl)-amine
sulfonyl)-benzene
hydrochloric acid
sulfonyl)-benzene
10 Bis-(β-(β-chloroethyl-
1-amino-4-allysulfonyl-
red
sulfonyl)-ethyl)-amine
benzene
hydrochloric acid
11 Bis-(β-(β-chloroethyl-
1-amino-5-(2,3-dibromo-
yellowish
sulfonyl)-ethyl)-amine
propionylamino)-benzene-2-
red
hydrochloric acid
sulfonic acid
12 Bis-(β-(β-chloroethyl-
1-amino-5-(2,3-dichloro-
yellowish
sulfonyl)-ethyl)-amine
propionylamino)-benzene-2-
red
hydrochloric acid
sulfonic acid
13 Bis-(β-(β-chloroethylsulfo-
1-amino-5-chloroacetyl-
yellowish
nyl)-ethyl)-amine hydro-
amino-benzene-2-sulfonic
red
chloride acid
14 Bis-(β-(β-chloroethylsulfo-
1-amino-3-(β-sulfatoethyl-
yellowish
nyl)-ethyl)-amine hydro-
sulfonyl)-benzene
red
chloride acid
15 3-(β-Chloroethylsulfonyl)-
1-amino-4-(β-sulfatoethyl-
red
propylamine hydrochloride
sulfonyl)-benzene
16 3-(β-Chloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
propylamine hydrochloride
sulfonyl)-benzene
red
17 3-(β-Chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl-
red
propylamine hydrochloride
sulfonyl)-benzene
18 3-(β-Chloroethylsulfonyl)-
1-amino-5-(2,3-dibromo-
yellowish
propylamine hydrochloride
propionylamino)-benzene-2-
red
sulfonic acid
19 4-(β-Chloroethylsulfonyl)-
1-amino-4-(β-sulfatoethyl-
red
butylamine hydrochloride
sulfonyl)-benzene
20 4-(β-Chloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
butylamine hydrochloride
sulfonyl)-benzene
red
21 4-(β-Chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl-
red
butylamine hydrochloride
sulfonyl)-benzene
22 4-(β-Chloroethylsulfonyl)-
1-amino-5-(2,3-dibromo-
yellowish
butylamine hydrochloride
propionylamino)-benzene-2-
red
sulfonic acid
23 β-(β-Chloroethylsulfonyl)-
1-amino-5-(4-(β-chloroethyl-
yellowish
ethylamine hydrochloride
sulfonyl)-butyrylamino)-
benzene-2-sulfonic acid
24 Bis-(β-(β-chloroethylsulfo-
1-amino-5-(4-β-chloroethyl-
yellowish
nyl)-ethyl)-amine hydro-
sulfonyl)-butyrylamino-
red
chloride benzene-2-sulfonic acid
__________________________________________________________________________
TABLE 2
__________________________________________________________________________
Hue on
No.
Amino compound
Diazo component
cotton
__________________________________________________________________________
1 β-(β-chloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
ethylamine hydrochloride
sulfonyl)-benzene
red
2 β-(β-chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl-
red
ethylamine hydrochloride
sulfonyl)-benzene
3 β-(β-chloroethylsulfonyl)-
1-amino-4-allysulfonyl-
red
ethylamine hydrochloride
benzene
4 β-(β-chloroethylsulfonyl)-
1-amino-5-(2,3-dibromopro-
yellowish
ethylamine hydrochloride
pionylamino)-benzene-2-
red
sulfonic acid
5 Bis-(β-(β-chloroethylsul-
1-amino-4-(β-sulfatoethyl-
red
fonyl)-ethyl)-amine
sulfonyl)-bezene
hydrochloride
6 Bis-(β-(β-chloroethylsul-
1-amino-2-(β-sulfatoethyl-
red
fonyl)-ethyl)-amine
sulfonyl)-benzene
hydrochloride
7 Bis-(β-(β-chloroethylsul-
1-amino-4-allysulfonyl-
red
fonyl)-ethyl)-amine
benzene
hydrochloride
8 Bis-(β-(β-chloroethylsul-
1-amino-5-(2,3-dibromo-
yellowish
fonyl)-ethyl)-amine
propionylamino)-benzene-
red
hydrochloride
2-sulfide acid
9 Bis-(Bβ-(β-chloroethysul-
1-amino-3-(β-sulfatoethyl-
yellowish
fonyl)-ethyl)-amine
sulfonyl)-benzene
red
hydrochloride
10 3-(βChloroethylsulfonyl)-
1-amino-4-(β-sulfatoethyl-
red
propylamine hydrochloride
sulfonyl)-benzene
11 3-(βChloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
propylamine hydrochloride
sulfonyl)-benzene
red
12 3-(β-Chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl-
red
propylamine hydrochloride
sulfonyl)-benzene
13 3-(β-Chloroethylsulfonyl)-
1-amino-5-(2,3-dibromo-
yellowish
propylamine hydrochloride
propionylamino)-benzene-2-
red
sulfonic acid
14 4-(β-Chloroethylsulfonyl)-
1-amino-4-(β-sulfatoethyl-
red
butylamine hydrochloride
sulfonyl)-benzene
15 4-(β-Chloroethylsulfonyl)-
1-amino-3-(β-sulfatoethyl-
yellowish
butylamine hydrochloride
sulfonyl)-benzene
red
16 4-(β-Chloroethylsulfonyl)-
1-amino-2-(β-sulfatoethyl
red
butylamine hydrochloride
sulfonyl)-benzene
17 4-(β-Chloroethylsulfonyl)-
1-amino-5-(2,3-dibromo-
yellowish
butylamine hydrochloride
propionylamino)-benzene-2-
red
sulfonic acid
18 β-(β-Chloroethylsulfonyl)-
1-amino-5-(4-(β-chloroethyl-
yellowish
ethylamine hydrochloride
sulfonyl)-butyrylamino)-
red
benzene-2-sulfonic acid
19 Bis-(β-(β-chloroethylsulfo-
1-amino-5-(4-(β-chloroethyl-
yellowish
nyl)-ethyl)-amine hydro-
sulfonyl)-butyrylamino)-
red
chloride benzene-2-sulfonic acid
__________________________________________________________________________
TABLE 3
__________________________________________________________________________
Hue on
No. Diazo component Diazo component cotton
__________________________________________________________________________
1 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-benzene amino)-4-chloro-6-(β-vinyl-
sulfonylethylamino)-1,3,5-
triazine
2 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4',6'-disulfo-
navy
sulfonyl)-benzene phenylamino)-4-chloro-6-
(β-vinylsulfonylethylamino)-
1,3,5-triazine
3 1-Amino-4-(β-sulfatoethyl-
2-(4'-amino-2',5'-disulfo-
greenish
sulfonyl)-benzene phenylamino)-4-chloro-6-
blue
(β-vinylsulfonylethylamino)-
1,3,5-triazine
4 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4',6'-disulfo-
navy
sulfonyl)-benzene phenylamino)-4-chloro-6-
(β-(β-chloroethylsulfonyl)-
ethylamino)-1,3,5-triazine
5 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-benzene amino)-4-chloro-6-(bis-(β-
vinylsulfonylethyl)-amino)-
1,3,5-triazine
6 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-benzene amino)-4-fluoro-6-(β-vinyl-
sulfonylethylamino)-1,3,5-
triazine
7 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
sulfonyl)-benzene amino)-4-fluoro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
8 1-Amino-4-(β-sulfatoethyl-
2-(4'-amino-2',5'-disulfophenyl-
greenish
sulfonyl)-benzene amino)-4-fluoro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
9 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
sulfonyl)-benzene amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
10 1-Amino-4-(β-sulfatoethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-benzene amino)-4-fluoro-6-(bis-(β-
vinylsulfonylethyl)-amino)-
1,3,5-triazine
11 1-Amino-3-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-chloro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
12 1-Amino-3-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
13 1-Amino-3-(β-sulfato-
2-(4'-amino-2',5'-disulfophenyl-
greenish
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
14 1-Amino-3-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
15 1-Amino-3-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-chloro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
16 1-Amino-3-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-fluoro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
17 1-Amino-3-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
18 1-Amino-3-(β-sulfato-
2-(4'-amino-2',5'-disulfophenyl-
greenish
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
19 1-Amino-3-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
20 1-Amino-3-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-fluoro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
21 1-Amino-2-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-chloro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
22 1-Amino-2-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
23 1-Amino-2-(β-sulfato-
2-(4'-amino-2',5'-disulfophenyl-
greenish
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
24 1-Amino-2-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-chloro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
25 1-Amino-2-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-chloro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
26 1-Amino-2-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-fluoro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
27 1-Amino-2-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
28 1-Amino-2-(β-sulfato-
2-(4'-amino-2',5'-disulfophenyl-
greenish
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
blue
nyl-ethylamino)-1,3,5-triazine
29 1-Amino-2-(β-sulfato-
2-(3'-amino-4',6'-disulfophenyl-
navy
ethylsulfonyl)-benzene
amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
30 1-Amino-2-(β-sulfato-
2-(3'-amino-4'-sulfophenylamino)-
navy
ethylsulfonyl)-benzene
4-fluoro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
31 1-Amino-4-allylsulfo-
2-(3'-amino-4'-sulfophenylamino)-
navy
nyl-benzene 4-chloro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
32 1-Amino-4-allylsulfo-
2-(3'-amino-4',6'-disulfophenyl-
navy
nyl-benzene amino)-4-chloro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
33 1-Amino-4-allylsulfo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
nyl-benzene amino)-4-chloro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
34 1-Amino-4-allylsulfo-
2-(3'-amino-4',6'-disulfophenyl-
navy
nyl-benzene amino)-4-chloro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
35 1-Amino-4-allylsulfo-
2-(3'-amino-4'-sulfophenylamino)-
navy
nyl-benzene 4-chloro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
36 1-Amino-4-allylsulfo-
2-(3'-amino-4'-sulfophenylamino)-
navy
nyl-benzene 4-fluoro-6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
37 1-Amino-4-allylsulfo-
2-(3'-amino-4',6'-disulfophenyl-
navy
nyl-benzene amino)-4-fluoro-6-(β-vinylsulfo-
nylethylamino)-1,3,5-triazine
38 1-Amino-4-allylsulfo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
nyl-benzene amine)-4-fluoro-6-(β-vinylsulfo-
blue
nylethylamino)-1,3,5-triazine
39 1-Amino-4-allylsulfo-
2-(3'-amino-4',6'-disulfophenyl-
navy
nyl-benzene amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
40 1-Amino-4-allylsulfo-
2-(3'-amino-4'-sulfophenylamino)-
navy
nyl-benzene 4-fluoro-6-(bis-(β-vinylsulfonyl-
ethyl)-amino)-1,3,5-triazine
41 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)- 4-chloro-6-(β-vinylsulfonylethyl-
benzene-2-sulfonic acid
amino)-1,3,5-triazine
42 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)- amino)-4-chloro-6-(β-vinylsulfo-
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
43 1-Amino-5-(2,3-dibromo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
propionylamino)- amino)-4-chloro-6-(β-vinylsulfo-
blue
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
44 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)- amino)-4-chloro-6-(β-(β-chloro-
benzene-2-sulfonic acid
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
45 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)- 4-chloro-6-(bis-(β-vinylsulfonyl-
benzene-2-sulfonic acid
ethyl)-amino)-1,3,5-triazine
46 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)- 4-fluoro-6-(β-vinylsulfonylethyl-
benzene-2-sulfonic acid
amino)-1,3,5-triazine
47 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)- amino)-4-fluoro-6-(β-vinylsulfo-
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
48 1-Amino-5-(2,3-dibromo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
propionylamino)- amino)-4-fluoro-6-(β-vinylsulfo-
blue
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
49 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)- amino)-4-fluoro-6-(β-(β-chloro-
benzene-2-sulfonic acid
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
50 1-Amino-5-(2,3-dibromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)- 4-fluoro-6-(bis-(β-vinylsulfonyl-
benzene-2-sulfonic acid
ethyl)-amino)-1,3,5-triazine
51 1-Amino-5-(α-bromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
acryloylamino)- 4-chloro-6-(β-vinylsulfonylethyl-
benzene-2-sulfonic acid
amino)-1,3,5-triazine
52 1-Amino-5-(α-bromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
acryloylamino)- amino)-4-chloro-6-(β-vinylsulfo-
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
53 1-Amino-5-(α-bromo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
acryloylamino)- amino)-4-chloro-6-(β-vinylsulfo-
blue
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
54 1-Amino-5-(α-bromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
acryloylamino)- amino)-4-chloro-6-(β-(β-chloro-
benzene-2-sulfonic acid
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
55 1-Amino-5-(α-bromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
acryloylamino)- 4-chloro-6-(bis-(β-vinylsulfonyl-
benzene-2-sulfonic acid
ethyl)-amino)-1,3,5-triazine
56 1-Amino-5-(α-bromo-
2-(3'-amino-4'-sulfophenylamino)-
navy
acryloylamino)- 4-fluoro-6-(β-vinylsulfonylethyl-
benzene-2-sulfonic acid
amino)-1,3,5-triazine
57 1-Amino-5-(α-bromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
acryloylamino)- amino)-4-fluoro-6-(β-vinylsulfo-
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
58 1-Amino-5-(α-bromo-
2-(4'-amino-2',5'-disulfophenyl-
greenish
acryloylamino)- amino)-4-fluoro-6-(β-vinylsulfo-
blue
benzene-2-sulfonic acid
nylethylamino)-1,3,5-triazine
59 1-Amino-5-(α-bromo-
2-(3'-amino-4',6'-disulfophenyl-
navy
acryloylamino)- amino)-4-fluoro-6-(β-(β-chloro
benzene-2-sulfonic acid
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
60 1-Amino-5-(αbromo
2-(3'-amino-4'-sulfophenylamino)-
navy
acryloylamino)- 4-fluoro-6-(bis-(β-vinylsulfonyl-
benzene-2-sulfonic acid
ethyl)-amino)-1,3,5-triazine
61 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)-benzene-
4-chloro-6-(β-vinylsulfonylethyl-
2-sulfonic acid amino)-1,3,5-triazine
62 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)-benzene-
amino)-4-chloro-6-(β-vinylsulfo-
2-sulfonic acid nylethylamino)-1,3,5-triazine
63 1-Amino-5-(2,3-dichloro-
2-(4'-amino-2',5'-disulfophenyl-
greenish
propionylamino)-benzene-
amino)-4-chloro-6-(β-vinylsulfo-
blue
2-sulfonic acid nylethylamino)-1,3,5-triazine
64 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)-benzene
amino)-4-chloro-6-(β-(β-chloro-
2-sulfonic acid ethylsulfonyl)-ethylamino)-
1,3,5-triazine
65 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)-benzene
4-chloro-6-(bis-(β-vinylsulfonyl-
2-sulfonic acid ethyl)-amino)-1,3,5-triazine
66 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)-benzene
4-fluoro-6-(β-vinylsulfonylethyl-
2-sulfonic acid amino)-1,3,5-triazine
67 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4'-disulfophenyl)-
navy
propionylamino)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
2-sulfonic acid nylethylamino)-1,3,5-triazine
68 1-Amino-5-(2,3-dichloro-
2-(4'-amino-2',5'-disulfophenyl-
greenish
propionylamino)-benzene
amino)-4-fluoro-6-(β-vinylsulfo-
blue
2-sulfonic acid nylethylamino)-1,3,5-triazine
69 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4',6'-disulfophenyl-
navy
propionylamino)-benzene
amino)-4-fluoro-6-(β-(β-chloro-
2-sulfonic acid ethylsulfonyl)-ethylamino)-
1,3,5-triazine
70 1-Amino-5-(2,3-dichloro-
2-(3'-amino-4'-sulfophenylamino)-
navy
propionylamino)-benzene
4-fluoro-6-(bis-(β-vinylsulfonyl-
2-sulfonic acid ethyl)-amino)-1,3,5-triazine
71 1-Amino-5-chloroacetyl-
2-(3'-amino-4'-sulfophenylamino)-
navy
amino-benzene-2-sulfo-
4-chloro-6-(β-vinylsulfonylethyl-
nic acid amino)-1,3,5-triazine
72 1-Amino-5-chloroacetyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
amino-benzene-2-sulfo-
amino)-4-chloro-6-(β-vinylsulfo-
nic acid nylethylamino)-1,3,5-triazine
73 1-Amino-5-chloroacetyl-
2-(4'-amino-2',5'-disulfophenyl-
greenish
amino-benzene-2-sulfo-
amino)-4-chloro-6-(β-vinylsulfo-
blue
nic acid nylethylamino)-1,3,5-triazine
74 1-Amino-5-chloroacetyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
amino-benzene-2-sulfo-
amino)-4-chloro-6-(β-(β-chloro-
nic acid ethylsulfonyl)-ethylamino)-
1,3,5-triazine
75 1-Amino-5-chloroacetyl-
2-(3'-amino-4'-sulfophenylamino)-
navy
amino-benzene-2-sulfo-
4-chloro-6-(bis-(β-vinylsulfonyl-
nic acid ethyl)-amino)-1,3,5-triazine
76 1-Amino-5-chloroacetyl-
2-(3'-amino-4'-sulfophenylamino)-
navy
amino-benzene-2-sulfo-
4-fluoro-6-(β-vinylsulfonylethyl-
nic acid amino)-1,3,5-triazine
77 1-Amino-5-chloroacetyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
amino-benzene-2-sulfo-
amino)-4-fluoro-6-(β-vinylsulfo-
nic acid nylethylamino)-1,3,5-triazine
78 1-Amino-5-chloroacetyl-
2-(4'-amino-2',5'-disulfophenyl-
greenish
amino-benzene-2-sulfo-
amino)-4-fluoro-6-(β-vinylsulfo-
blue
nic acid nylethylamino)-1,3,5-triazine
79 1-Amino-5-chloroacetyl-
2-(3'-amino-4',6'-disulfophenyl-
navy
amino-benzene-2-sulfo-
amino)-4-fluoro-6-(β-(β-chloro-
nic acid ethylsulfonyl)-ethylamino)-
1,3,5-triazine
80 1-Amino-5-chloroacetyl-
2-(3'-amino-4'-sulfophenylamino)-
navy
amino-benzene-2-sulfo-
4-fluoro-6-(bis-(β-vinylsulfonyl-
nic acid ethyl)-amino)-1,3,5-triazine
81 2-(3'-Amino-4',6'-disulfo-
1-amino-4-(β-sulfatoethylsulfo-
greenish
nylamino-4-chloro-6-(β-
nyl)-benzene blue
vinylsulfonylethylamino)-
1,3,5-triazene
82 2-(4'-Amino-2',5'-disulfo-
1-amino-4-(β-sulfatoethylsulfo-
greenish
phenylamino)-4-chloro-6-
nyl)-benzene blue
(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
83 2-(3'-Amino-4',6'-disulfo-
1-amino-4-(β-sulfatoethyl-
greenish
phenylamino)-4-chloro-6-
sulfonyl)-benzene blue
(β-(β-chloroethylsulfonyl)-
ethylamino)-1,3,5-triazine
84 2-(3'-Amino-4'-sulfophenyl)-
1-amino-4-(β-sulfatoethyl-
greenish
amino)-4-chloro-6-(bis-(β-
sulfonyl)-benzene blue
vinylsulfonylethyl)-amino)-
1,3,5-triazine
85 2-(3'-Amino-4' -sulfophenyl-
1-amino-4-(β-sulfatoethyl-
greenish
amino)-4-fluoro-6-(β-vinyl-
sulfonyl)-benzene blue
sulfonylethylamino)-1,3,5-
triazine
86 2-(3'-Amino-4',6'-disulfo-
1-amino-4-(β-sulfatoethyl-
greenish
phenylamino)-4-fluoro-6-(β-
sulfonyl)-benzene blue
vinylsulfonylethylamino)-
1,3,5-triazine
87 2-(4'-Amino-2',5'-disulfo-
1-amino-4-(β-sulfatoethyl-
greenish
phenylamino)-4-fluoro-6-(β-
sulfonyl)-benzene blue
vinylsulfonylethylamino)-
1,3,5-triazine
88 2-(3'-Amino-4',6'-disulfo-
1-amino-4-(β-sulfatoethyl-
greenish
phenylamino)-4-fluoro-6-(β-
sulfonyl)-benzene blue
(β-chloroethylsulfonyl)-
ethylamino)-1,3,5-triazine
89 2-(3'-Amino-4'-sulfophenyl-
1-amino-4-(β-sulfatoethyl-
greenish
amino)-4-fluoro-6-(bis(β-
sulfonyl)-benzene blue
vinylsulfonylethyl)-amino)-
1,3,5-triazine
90 2-(3'-Amino-4'-sulfophenyl-
1-amino-3-( -sulfatoethyl-
greenish
amino)-4-chloro-6-(β-vinyl-
sulfonyl)-benzene blue
sulfonylethylamino)-1,3,5-
triazine
91 2-(3'-Amino-4',6'-disulfophe-
1-amino-3-( -sulfatoethyl-
greenish
nylamino)-4-chloro-6-(β-
sulfonyl)-benzene blue
vinylsulfonylethylamino)-
1,3,5-triazine
92 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-3-( -sulfatoethyl-
greenish
amino)-4-chloro-6-(β-vinylsulfo-
sulfonyl)-benzene blue
nylethylamino)-1,3,5-triazine
93 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-3-(β-sulfato-
greenish
amino)-4-chloro-6-(β-(β-chloro-
ethylsulfonyl)-benaene
blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
94 2-(3'-Amino-4'-sulfophenyl-
1-amino-3-(β-sulfato-
greenish
amino)-4-chloro-6-(bis(β-vinyl-
ethylsulfonyl)-benaene
blue
sulfonylethyl)-amino)-1,3,5-triazine
95 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-3-(β-sulfato-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
ethylsulfonyl)-benaene
blue
amino)-1,3,5-triazine
96 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-3-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-vinylsulfo-
ethylsulfonyl)-benaene
blue
nylethylamino)-1,3,5-triazine
97 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-3-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-vinylsulfo-
ethylsulfonyl)-benaene
blue
nylethylamino)-1,3,5-triazine
98 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-3-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-benaene
blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
99 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-3-(β-sulfato-
greenish
4-fluoro-6-(bis(β-vinylsulfonyl-
ethylsulfonyl)-benaene
blue
ethyl)-amino)-1,3,5-triazine
100 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-2-(β-sulfato-
greenish
4-chloro-6-(β-vinylsulfonylethyl-
ethylsulfonyl)-benzene
blue
amino)-1,3,5-triazine
101 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-chloro-6-(β-vinylsulfo-
ethylsulfonyl)-benzene
blue
nylethylamino)-1,3,5-triazine
102 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
ethylsulfonyl)-benzene
blue
ethylamino)-1,3,5-triazine
103 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-chloro-6-(β-(β-chloro-
ethylsulfonyl)-benzene
blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
104 2-(3'-Amino-4'-sulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-chloro-6-(bis-(β-vinyl-
ethylsulfonyl)-benzene
blue
sulfonylethyl)-amino)-1,3,5-triazine
105 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-2-(β-sulfato-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
ethylsulfonyl)-benzene
blue
amino)-1,3,5-triazine
106 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-vinylsulfo-
ethylsulfonyl)-benzene
blue
nylethylamino)-1,3,5-triazine
107 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-vinylsulfo-
ethylsulfonyl)-benzene
blue
nylethylamino)-1,3,5-triazine
108 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-2-(β-sulfato-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-benzene
blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
109 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-2-(β-sulfato-
greenish
4-fluoro-6-(bis-(β-vinylsulfonyl-
ethylsulfonyl)-benzene
blue
ethyl)-amino)-1,3,5-triazine
110 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-4-allylsulfo-
greenish
4-chloro-6-(β-vinylsulfonylethyl-
nyl benzene blue
amino)-1,3,5-triazine
111 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
nyl benzene blue
ethylamino)-1,3,5-triazine
112 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-chloro-6-(β-vinylsulfo-
nyl benzene blue
nylethylamino)-1,3,5-triazine
113 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-chloro-6-(β-(β-chloro-
nyl benzene blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
114 2-(3'-Amino-4'-sulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-chloro-6-(bis-(β-vinyl-
nyl benzene blue
sulfonylethyl)-amino)-1,3,5-triazine
115 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-4-allylsulfo-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
nyl benzene blue
amino)-1,3,5-triazine
116 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
nyl benzene blue
ethylamino)-1,3,5-triazine
117 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
nyl benzene blue
ethylamino)-1,3,5-triazine
118 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-4-allylsulfo-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
nyl benzene blue
ethylsulfonyl)-ethylamino)-
1,3,5-triazine
119 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-4-allylsulfo-
greenish
4-fluoro-6-(bis(β-vinylsulfonyl-
nyl benzene blue
ethyl)-amino)-1,3,5-triazine
120 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-dibromo-
greenish
4-chloro-6-(β-vinylsulfonylethyl-
propionylamino)-benzene-
blue
amino)-1,3,5-triazine
2-sulfonic acid
121 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-chloro-6-(β-vinylsulfo-
propionylamino)-benzene-
blue
nylethylamino)-1,3,5-triazine
2-sulfonic acid
122 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
propionylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
123 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-chloro-6-(β-(β-chloro-
propionylamino)-benzene-
blue
ethylsulfonyl)-ethylamino)-
2-sulfonic acid
1,3,5-triazine
124 2-(3'-Amino-4'-sulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-chloro-6-(bis-(β-vinyl-
propionylamino)-benzene-
blue
sulfonylethyl)-amino)-1,3,5-triazine
2-sulfonic acid
125 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-dibromo-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
propionylamino)-benzene-
blue
amino)-1,3,5-triazine
2-sulfonic acid
126 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
propionylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
127 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
propionylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
128 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-dibromo-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
propionylamino)-benzene-
blue
ethylsulfonyl)-ethylamino)-1,3,5-
2-sulfonic acid
triazine
129 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-dibromo-
greenish
4-fluoro-6-(bis-(β-vinylsulfonyl-
propionylamino)-benzene-
blue
ethyl)-amino)-1,3,5-triazine
2-sulfonic acid
130 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(α-bromo-
greenish
4-chloro-6-(β-vinylsulfonylethyl-
acryloylamino)-benzene-
blue
amino)-1,3,5-triazine
2-sulfonic acid
131 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
acryloylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
132 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
acryloylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
133 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-chloro-6-(β-(β-chloro-
acryloylamino)-benzene-
blue
ethylsulfonyl)-ethylamino)-1,3,5-
2-sulfonic acid
triazine
134 2-(3'-Amino-4'-sulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-chloro-6-(bis-(β-vinyl-
acryloylamino)-benzene-
blue
sulfonylethyl)-amino)-1,3,5-triazine
2-sulfonic acid
135 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(α-bromo-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
acryloylamino)-benzene-
blue
amino)-1,3,5-triazine
2-sulfonic acid
136 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
acryloylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
137 2-(4' -Amino-2',5'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
acryloylamino)-benzene-
blue
ethylamino)-1,3,5-triazine
2-sulfonic acid
138 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(α-bromo-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
acryloylamino)-benzene-
blue
ethylsulfonyl)-ethylamino)-1,3,5-
2-sulfonic acid
triazine
139 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(α-bromo-
greenish
4-fluoro-6-(bis(β-vinylsulfonyl-
acryloylamino)-benzene-
blue
ethyl)-amino)-1,3,5-triazine
2-sulfonic acid
140 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-di- greenish
4-chloro-6-(βvinylsulfonylethyl-
chloropropionylamino)-
blue
amino)-1,3,5-triazine
benzene-2-sulfonic acid
141 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-chloro-6-(β-vinylsulfo-
chloropropionylamino)-
blue
nylethylamino)-1,3,5-triazine
benzene-2-sulfonic acid
142 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
chloropropionylamino)-
blue
ethylamino)-1,3,5-triazine
benzene-2-sulfonic acid
143 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-chloro-6-(β-(β-chloro-
chloropropionylamino)-
blue
ethylsulfonyl)-ethylamino)-1,3,5-
benzene-2-sulfonic acid
triazine
144 2-(3'-Amino-4'-sulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-chloro-6-(bis-(β-vinyl-
chloropropionylamino)-
blue
sulfonylethyl)-amino)-1,3,5-triazine
benzene-2-sulfonic acid
145 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-di- greenish
4-fluoro-6-(β-vinylsulfonylethyl-
chloropropionylamino)-
blue
amino)-1,3,5-triazine
benzene-2-sulfonic acid
146 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
chloropropionylamino)-
blue
ethylamino)-1,3,5-triazine
benzene-2-sulfonic acid
147 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
chloropropionylamino)-
blue
ethylamino)-1,3,5-triazine
benzene-2-sulfonic acid
148 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(2,3-di- greenish
amino)-4-fluoro-6-(β-(β-chloro-
chloropropionylamino)-
blue
ethylsulfonyl)-ethylamino)-1,3,5-
benzene-2-sulfonic acid
triazine
149 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(2,3-di- greenish
4-fluoro-6-(bis-(β-vinylsulfonyl-
chloropropionylamino)-
blue
ethyl)-amino)-1,3,5-triazine
benzene-2-sulfonic acid
150 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-chloroacetyl-
greenish
4-chloro-6-(β-vinylsulfonylethyl-
amino-benzene-2- blue
amino)-1,3,5-triazine
sulfonic acid
151 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
amino-benzene-2- blue
ethylamino)-1,3,5-triazine
sulfonic acid
152 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-chloro-6-(β-vinylsulfonyl-
amino-benzene-2- blue
ethylamino)-1,3,5-triazine
sulfonic acid
153 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-chloro-6-(β-(β-chloro-
amino-benzene-2- blue
ethylsulfonyl)-ethylamino)-1,3,5-
sulfonic acid
triazine
154 2-(3'-Amino-4'-sulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-chloro-6-(bis-(β-vinyl-
amino-benzene-2- blue
sulfonylethyl)-amino)-1,3,5-
sulfonic acid
triazine
155 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-chloroacetyl-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
amino-benzene-2- blue
amino)-1,3,5-triazine
sulfonic acid
156 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-fluoro-6-(β -vinylsulfonyl-
amino-benzene-2- blue
ethylamino)-1,3,5-triazine
sulfonic acid
157 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-fluoro-6-(β-vinylsulfonyl-
amino-benzene-2- blue
ethylamino)-1,3,5-triazine
sulfonic acid
158 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-chloroacetyl-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
amino-benzene-2- blue
ethylsulfonyl)-ethylamino)-1,3,5-
sulfonic acid
triazine
159 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-chloroacetyl-
greenish
4-fluoro-6-(bis-(β-vinylsulfonyl-
amino-benzene-2- blue
ethyl)-amino)-1,3,5-triazine
sulfonic acid
160 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4'-sulfophe-
navy
sulfonyl)-butyrylamino)-benzene-
nylamino)-4-chloro-6-(β-
2-sulfonic acid vinylsulfonylethylamino)-
1,3,5-triazine
161 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4',6'-disulfo-
navy
sulfonyl)-butyrylamino)-benzene-
phenylamino)-4-chloro-6-
2-sulfonic acid (β-vinylsulfonylethyl-
amino)-1,3,5-triazine
162 1-Amino-5-(4-(β-chloroethyl-
2-(4'-amino-2',5'-disul-
greenish
sulfonyl)-butyrylamino)-benzene-
fophenylamino)-4-chloro-
blue
2-sulfonic acid 6-(β-vinylsulfonylethyl-
amino)-1,3,5-triazine
163 1-Amino-5-(4-(β-chloroethyl-
2-(3'-Amino-4',6'-disul-
navy
sulfonyl)-butyrylamino)-benzene-
fophenylamino)-4-chloro-
2-sulfonic acid 6-(β-(β-chloroethylsulfo-
nyl)-ethylamino)-1,3,5-
triazine
164 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-butyrylamino)-ben-
amino)-4-chloro-6-(bis-(β-
zene-2-sulfonic acid
vinylsulfonylethyl)-amino)-
1,3,5-triazine
165 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-butyrylamino)-ben-
amino)-4-fluoro-6-(β-vinyl-
zene-2-sulfonic acid
sulfonylethylamino)-1,3,5-
triazine
166 1-Amino-5-(4-(β -chloroethyl-
2-(3'-amino-4',6'-disulfo-
navy
sulfonyl)-butyrylamino)-ben-
phenylamino)-4-fluoro-6-(β-
zene-2-sulfonic acid
vinylsulfonylethylamino)-
1,3,5-triazine
167 1-Amino-5-(4-(β-chloroethyl-
2-(4'-amino-2',5'-disulfo-
greenish
sulfonyl)-butyrylamino)-ben-
phenylamino)-4-fluoro-6-(β-
blue
zene-2-sulfonic acid
vinylsulfonylethylamino)-
1,3,5-triazine
168 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4',6'-disulfo-
navy
sulfonyl)-butyrylamino)-ben-
phenylamino)-4-fluoro-6-(β-(β-
zene-2-sulfonic acid
chloroethylsulfonyl)-ethyl-
amino)-1,3,5-triazine
169 1-Amino-5-(4-(β-chloroethyl-
2-(3'-amino-4'-sulfophenyl-
navy
sulfonyl)-butyrylamino)-
amino)-4-fluoro-6-(bis-(β-
benzene-2-sulfonic acid
vinylsulfonylethyl)-amino)-
1,3,5-triazine
170 2-(3'-Amino-4'-sulfophenyl-
1-Amino-5-(4-(β-chloroethyl-
greenish
amino)-4-chloro-6-(β-vinyl-
sulfonyl)-butyrylamino)-
blue
sulfonylethylamino)-1,3,5-
benzene-2-sulfonic acid
triazine
171 2-(3'-Amino-4',6'-disulfo-
1-Amino-5-(4-(β-chloroethyl-
greenish
phenylamino)-4-chloro-6-(β-
sulfonyl)-butyrylamino)-
blue
vinylsulfonylethylamino)-
benzene-2-sulfonic acid
1,3,5-triazine
172 2-(4'-Amino-2',5'-disulfo-
1-Amino-5-(4-(β-chloroethyl-
greenish
phenylamino)-4-chloro-6-(β-
sulfonyl)-butyrylamino)-
blue
vinylsulfonylethylamino)-
benzene-2-sulfonic acid
1,3,5-triazine
173 2-(3'-Amino-4',6'-disulfo-
1-Amino-5-(4-(β-chloroethyl-
greenish
phenylamino)-4-chloro-6-(β-
sulfonyl)-butyrylamino)-
blue
(β-chloroethylsulfonyl)-ethyl-
benzene-2-sulfonic acid
amino)-1,3,5-triazine
174 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(4-(β-chloro-
greenish
4-chloro-6-(bis-(β-vinylsulfonyl-
ethylsulfonyl)-butyryl-
blue
ethyl)-amino)-1,3,5-triazine
amino)-benzene-2-
sulfonic acid
175 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(4-(β-chloro-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
ethylsulfonyl)-butyryl-
blue
amino)-1,3,5-triazine
amino)-benzene-2-
sulfonic acid
176 2-(3'-Amino-4',6'-disulfophenylamino-
1-amino-5-(4-(β-chloro-
greenish
4-fluoro-6-(β-vinylsulfonylethyl-
ethylsulfonyl)-butyryl-
blue
amino)-1,3,5-triazine
amino)-benzene-2-
sulfonic acid
177 2-(4'-Amino-2',5'-disulfophenyl-
1-amino-5-(4-(β-chloro-
greenish
amino)-4-fluoro-6-(β-vinylsulfo-
ethylsulfonyl)-butyryl-
blue
nylethylamino)-1,3,5-triazine
amino)-benzene-2-
sulfonic acid
178 2-(3'-Amino-4',6'-disulfophenyl-
1-amino-5-(4-(β-chloro-
greenish
amino)-4-fluoro-6-(β-(β-chloro-
ethylsulfonyl)-butyryl-
blue
ethylsulfonyl)-ethylamino)-
amino)-benzene-2-sulfo-
1,3,5-triazine nic acid
179 2-(3'-Amino-4'-sulfophenylamino)-
1-amino-5-(4-(β-chloro-
greenish
4-fluoro-6-(bis-(β-vinylsulfonyl-
ethylsulfonyl)-butyryl-
blue
ethyl)-amino)-1,3,5-triazine
amino)-benzene-2-sulfo-
nic acid
__________________________________________________________________________
TABLE 4
______________________________________
Hue on
No. Intermediate cotton
______________________________________
1 2-Amino-5-hydroxynaphthalene-7-sulfonic
orange
acid
2 2-Methylamino-5-hydroxynaphthalene-7-
orange
sulfonic acid
3 3-Amino-5-hydroxynaphthalene-7-sulfonic
red
acid
______________________________________
TABLE 5
______________________________________
Hue on
No. Intermediate cotton
______________________________________
1 2-Amino-5-hydroxynaphthalene-7-sulfonic
orange
acid
2 2-Methylamino-5-hydroxynaphthalene-7-
orange
sulfonic acid
3 3-Amino-5-hydroxynaphthalene-7-sulfonic
red
acid
______________________________________
Claims (10)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH579583 | 1983-10-26 | ||
| CH5795/83 | 1983-10-26 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06833427 Continuation | 1986-02-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4908436A true US4908436A (en) | 1990-03-13 |
Family
ID=4299432
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/921,849 Expired - Lifetime US4908436A (en) | 1983-10-26 | 1986-10-23 | Fibre-reactive azo dyes containing vinylsulfonyl groups and further aliphatic fibre-reactive radicals |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4908436A (en) |
| EP (1) | EP0141367B1 (en) |
| JP (1) | JPS60110761A (en) |
| DE (1) | DE3470169D1 (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5092903A (en) * | 1989-09-22 | 1992-03-03 | Ciba-Geigy Corporation | Process for dyeing or printing blends of cellulosic fibre materials and silk with dihalo-propionamido or halo-acryl amido reactive dyes |
| US5093481A (en) * | 1987-12-01 | 1992-03-03 | Bayer Aktiengesellschaft | Fiber reactive azo dyestuffs |
| US5112959A (en) * | 1989-06-01 | 1992-05-12 | Sumitomo Chemical Company, Limited | Polyazo dye compounds having plural vinylsulfone type fiber reactive groups in one molecule |
| US5138041A (en) * | 1989-01-04 | 1992-08-11 | Hoechst Aktiengesellschaft | Water-soluble fiber-reactive monoazo and disazo dyestuffs having a s-triazinylamino group and three fiber-reactive groups of the vinylsulfone series |
| US5243034A (en) * | 1988-12-21 | 1993-09-07 | Hoechst Aktiengesellschaft | Disazo dyestuffs having a triazine moiety and a fiberreactive group of vinylsulfone series |
| US5597902A (en) * | 1992-05-04 | 1997-01-28 | Bayer Aktiengesellschaft | Bi -and polyfunctional reactive dyestuffs, their prepartion and their use |
| US5637705A (en) * | 1993-02-04 | 1997-06-10 | Sumitomo Chemical Company, Limited | Bisazo compounds and use thereof as fiber reactive dyes |
| US5831040A (en) * | 1996-06-14 | 1998-11-03 | Ciba Specialty Chemicals Corporation | Disazo reactive dyes, their preparation and use |
| US5952476A (en) * | 1998-08-21 | 1999-09-14 | Everlight Usa, Inc. | Red reactive dyestuffs |
| US6624291B2 (en) | 2000-07-25 | 2003-09-23 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Yellow-reactive monoazo dyes containing a tertiary or a quarternary nitrogen group, methods for their preparation and use thereof for dyeing hydroxy-and/or carboxamido-containing fiber material |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3767312D1 (en) * | 1986-01-10 | 1991-02-21 | Ciba Geigy Ag | REACTIVE DYES, THEIR PRODUCTION AND USE. |
| DE3843014A1 (en) * | 1988-12-21 | 1990-06-28 | Hoechst Ag | WATER-SOLUBLE DYES, METHOD FOR THEIR PRODUCTION AND THEIR USE |
| CN102391671B (en) * | 2011-06-29 | 2016-07-13 | 天津德凯化工股份有限公司 | A kind of nylon orange reactive dye and preparation method thereof |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1007752A (en) * | 1961-05-06 | 1965-10-22 | Farbwerke Hoechst Aktiengesellschaft | |
| US3998805A (en) * | 1973-04-04 | 1976-12-21 | Ciba-Geigy Corporation | Sulphatoethylene (sulphonyl or sulphonylamino) phenyleneazo dyestuffs |
| GB1576237A (en) * | 1976-04-03 | 1980-10-01 | Cassella Ag | Dyestuffs containing the triazine ring their preparation and use |
| EP0065732A1 (en) * | 1981-05-21 | 1982-12-01 | Hoechst Aktiengesellschaft | Water soluble disazo compounds, process for their preparation and their use as dyestuffs |
| EP0074928A2 (en) * | 1981-09-16 | 1983-03-23 | Ciba-Geigy Ag | Reactive dyestuffs, their preparation and their use |
| EP0094055A1 (en) * | 1982-05-12 | 1983-11-16 | Hoechst Aktiengesellschaft | Monoazo compounds, process for their preparation and their use as dyestuffs |
| US4622390A (en) * | 1980-09-06 | 1986-11-11 | Hoechst Aktiengesellschaft | Water-soluble disazo compounds containing an amino naphthol-disulfonic acid moiety as a coupling component and fibre-reactive groups |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0070808B1 (en) * | 1981-07-21 | 1986-08-27 | Ciba-Geigy Ag | Reactive dyestuffs, their preparation and their use |
-
1984
- 1984-10-23 EP EP84112760A patent/EP0141367B1/en not_active Expired
- 1984-10-23 DE DE8484112760T patent/DE3470169D1/en not_active Expired
- 1984-10-26 JP JP59225644A patent/JPS60110761A/en active Granted
-
1986
- 1986-10-23 US US06/921,849 patent/US4908436A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1007752A (en) * | 1961-05-06 | 1965-10-22 | Farbwerke Hoechst Aktiengesellschaft | |
| US3998805A (en) * | 1973-04-04 | 1976-12-21 | Ciba-Geigy Corporation | Sulphatoethylene (sulphonyl or sulphonylamino) phenyleneazo dyestuffs |
| GB1576237A (en) * | 1976-04-03 | 1980-10-01 | Cassella Ag | Dyestuffs containing the triazine ring their preparation and use |
| US4622390A (en) * | 1980-09-06 | 1986-11-11 | Hoechst Aktiengesellschaft | Water-soluble disazo compounds containing an amino naphthol-disulfonic acid moiety as a coupling component and fibre-reactive groups |
| EP0065732A1 (en) * | 1981-05-21 | 1982-12-01 | Hoechst Aktiengesellschaft | Water soluble disazo compounds, process for their preparation and their use as dyestuffs |
| EP0074928A2 (en) * | 1981-09-16 | 1983-03-23 | Ciba-Geigy Ag | Reactive dyestuffs, their preparation and their use |
| EP0094055A1 (en) * | 1982-05-12 | 1983-11-16 | Hoechst Aktiengesellschaft | Monoazo compounds, process for their preparation and their use as dyestuffs |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5093481A (en) * | 1987-12-01 | 1992-03-03 | Bayer Aktiengesellschaft | Fiber reactive azo dyestuffs |
| US5243034A (en) * | 1988-12-21 | 1993-09-07 | Hoechst Aktiengesellschaft | Disazo dyestuffs having a triazine moiety and a fiberreactive group of vinylsulfone series |
| US5138041A (en) * | 1989-01-04 | 1992-08-11 | Hoechst Aktiengesellschaft | Water-soluble fiber-reactive monoazo and disazo dyestuffs having a s-triazinylamino group and three fiber-reactive groups of the vinylsulfone series |
| US5112959A (en) * | 1989-06-01 | 1992-05-12 | Sumitomo Chemical Company, Limited | Polyazo dye compounds having plural vinylsulfone type fiber reactive groups in one molecule |
| US5092903A (en) * | 1989-09-22 | 1992-03-03 | Ciba-Geigy Corporation | Process for dyeing or printing blends of cellulosic fibre materials and silk with dihalo-propionamido or halo-acryl amido reactive dyes |
| US5597902A (en) * | 1992-05-04 | 1997-01-28 | Bayer Aktiengesellschaft | Bi -and polyfunctional reactive dyestuffs, their prepartion and their use |
| US5686642A (en) * | 1992-05-04 | 1997-11-11 | Bayer Aktiengesellschaft | Compounds useful for the preparation of bi-and polyfunctional reactive dyestuffs |
| US5637705A (en) * | 1993-02-04 | 1997-06-10 | Sumitomo Chemical Company, Limited | Bisazo compounds and use thereof as fiber reactive dyes |
| US5831040A (en) * | 1996-06-14 | 1998-11-03 | Ciba Specialty Chemicals Corporation | Disazo reactive dyes, their preparation and use |
| MY120699A (en) * | 1996-06-14 | 2005-11-30 | Ciba Sc Holding Ag | Reactive dyes, their preparation and use |
| US5952476A (en) * | 1998-08-21 | 1999-09-14 | Everlight Usa, Inc. | Red reactive dyestuffs |
| US6624291B2 (en) | 2000-07-25 | 2003-09-23 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Yellow-reactive monoazo dyes containing a tertiary or a quarternary nitrogen group, methods for their preparation and use thereof for dyeing hydroxy-and/or carboxamido-containing fiber material |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3470169D1 (en) | 1988-05-05 |
| JPS6338071B2 (en) | 1988-07-28 |
| EP0141367A1 (en) | 1985-05-15 |
| JPS60110761A (en) | 1985-06-17 |
| EP0141367B1 (en) | 1988-03-30 |
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